High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age (2012)
- Authors:
- Autor USP: ROSENBERG, CARLA - IB
- Unidade: IB
- Subjects: DOENÇAS GENÉTICAS; CROMOSSOMOS (ANOMALIAS)
- Language: Inglês
- Imprenta:
- Source:
- Título: European Society for Paediatric Endocrinology (ESPE)
- Volume/Número/Paginação/Ano: v. 78, n. suppl. 1, Sep. p. 98, P1-d2-316, 2012
- Conference titles: Annual Meeting of the European Society for Paediatric Endocrinology (ESPE)
-
ABNT
CANTON, Ana e RODRIGUES, Tatiane e ROSENBERG, Carla. High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age. European Society for Paediatric Endocrinology (ESPE). Bristol: Instituto de Biociências, Universidade de São Paulo. Disponível em: http://www.karger.com/Article/Pdf/343182. Acesso em: 11 out. 2024. , 2012 -
APA
Canton, A., Rodrigues, T., & Rosenberg, C. (2012). High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age. European Society for Paediatric Endocrinology (ESPE). Bristol: Instituto de Biociências, Universidade de São Paulo. Recuperado de http://www.karger.com/Article/Pdf/343182 -
NLM
Canton A, Rodrigues T, Rosenberg C. High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age [Internet]. European Society for Paediatric Endocrinology (ESPE). 2012 ; 78( suppl. 1): Se 98.[citado 2024 out. 11 ] Available from: http://www.karger.com/Article/Pdf/343182 -
Vancouver
Canton A, Rodrigues T, Rosenberg C. High frequency of submicroscopic chromosomal deletions and duplications in dysmorphic patients born small for gestational age [Internet]. European Society for Paediatric Endocrinology (ESPE). 2012 ; 78( suppl. 1): Se 98.[citado 2024 out. 11 ] Available from: http://www.karger.com/Article/Pdf/343182 - Number of rare germline CNVs and TP53 mutation types
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